Hossein Darvish

3.6k citations

96 papers · 1.3k indexed · h-index 18

Neurology top 5%
- Parkinson's Disease Mechanisms and Treatments 10
Neurology top 10%
- Parkinson's Disease Mechanisms and Treatments 10
Cellular and Molecular Neuroscience top 5%
Cell Biology top 10%
Genetics top 10%
- Genetics and Neurodevelopmental Disorders 22
- Genomics and Rare Diseases 10
- Genomic variations and chromosomal abnormalities 9
Cognitive Neuroscience
- Autism Spectrum Disorder Research 12
Molecular Biology
- RNA Research and Splicing 9
- RNA regulation and disease 7
- RNA and protein synthesis mechanisms 6

Co-authors: Coro Paisán‐Ruiz Mina Ohadi Abbas Tafakhori Gholam Ali Shahidi Babak Emamalizadeh Javad Jamshidi Siamak Karkheiran Ruth H. Walker
Cited by: Neurology Cellular and Molecular Neuroscience
Partner nations: Iran United States Germany

In The Last Decade

Hossein Darvish

93 papers receiving 1.3k citations

Peers

Countries citing papers authored by Hossein Darvish

Since Specialization

Citations

This map shows the geographic impact of Hossein Darvish's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Hossein Darvish with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Hossein Darvish more than expected).

Fields of papers citing papers by Hossein Darvish

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Hossein Darvish. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Hossein Darvish. The network helps show where Hossein Darvish may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Hossein Darvish, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Hossein Darvish Line = papers co-authored together Hossein Darvish links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	A biallelic loss-of-function variant in TMEM147 causes profound intellectual disability and spasticity Tahereh Ghorashi,Hossein Darvish,Somayeh Bakhtiari,Abbas Tafakhori,Michael C. Kruer,Hossein Mozdarani	2023	0
2	A novel mutation in the ALS2 gene in an iranian kurdish family with juvenile amyotrophic lateral sclerosis Yousef Daneshmandpour,Zahra Bahmanpour,Somayeh Kazeminasab,Ehsan Aghaei Moghadam,Elham Alehabib,Marjan Chapi,Abbas Tafakhori,Negar Aghaei,Hossein Darvish,Babak Emamalizadeh	2022	2
3	Mutational analysis of CYP1B1 gene in Iranian pedigrees with glaucoma reveals known and novel mutations Babak Emamalizadeh,Yousef Daneshmandpour,Somayeh Kazeminasb,Ehsan Aghaei Moghadam,Zahra Bahmanpour,Elham Alehabib,Somayeh Alinaghi,Azadeh Doozandeh,Minoo Atakhorrami,Hossein Darvish	2021	3
4	Clinical and molecular spectrum of P/Q type calcium channel Cav2.1 in epileptic patients Elham Alehabib,Zahra Esmaeilizadeh,Sakineh Ranji‐Burachaloo,Abbas Tafakhori,Hossein Darvish,Abolfazl Movafagh	2021	8
5	ANXA1 with Anti‐Inflammatory Properties Might Contribute to Parkinsonism Hossein Darvish,Luís Azcona,Shaghayegh Taghavi,Saghar Ghasemi Firouzabadi,Abbas Tafakhori,Elham Alehabib,Fatemeh Mohajerani,Safoura Zardadi,Coro Paisán‐Ruiz	2021	8
6	The phenotypic spectrum of PCDH12 associated disorders - Five new cases and review of the literature Walid Fazeli,Daniel Bamborschke,Abubakar Moawia,Somayeh Bakhtiari,Abbas Tafakhori,Matthias Giersdorf,Andreas Hahn,Anja Weik,Kirsten Kolzter,Sajad Shafiee,Sheng Chih Jin,Friederike Körber,Min Ae Lee‐Kirsch,Hossein Darvish,Sebahattin Çırak,Michael C. Kruer,Anne Koy	2021	5
7	Incomplete penetrance of MITF gene c.943C>T mutation in an extended family with Waardenburg syndrome type II Elham Alehabib,Somayeh Alinaghi,Fatemeh Pourfatemi,Hossein Darvish	2020	6
8	Analysis of polymorphism and function of GA repeat in RIT2 gene promoterAnalysis of polymorphism and function of GA repeat in RIT2 gene promoter in Parkinson’s disease Babak Emamalizadeh,Mina Ohadi,Hossein Darvish,Azade Rakhshan,Abolfazl Movafagh,ُSُheikhpour Mojgan	2020	1
9	A novel splice site mutation in the SDCCAG8 gene in an Iranian family with Bardet–Biedl syndrome Zahra Bahmanpour,Yousef Daneshmandpour,Somayeh Kazeminasab,Soudabeh Khalil Khalili,Elham Alehabib,Marjan Chapi,Mohsen Soosanabadi,Hossein Darvish,Babak Emamalizadeh	2020	5
10	Features, genetics and their correlation in Jalili syndrome: a systematic review Yousef Daneshmandpour,Hossein Darvish,Fariba Pashazadeh,Babak Emamalizadeh	2019	11
11	Whole-exome sequencing identified a novel mutation of MLH1 in an extended family with lynch syndrome Hamid Ghaedi,Samira Molaei Ramshe,Maryam Omidvar,Labbaf Afsaneh,Elham Alehabib,Sanaz Akbari,Fatemeh Pourfatemi,Hossein Darvish	2019	2
12	Molecular characterization of PRKN structural variations identified through whole‐genome sequencing Paloma Bravo,Hossein Darvish,Abbas Tafakhori,Luís Azcona,Amir Hossein Johari,Faezeh Jamali,Coro Paisán‐Ruiz	2018	6
13	RIT2: responsible and susceptible gene for neurological and psychiatric disorders Yousef Daneshmandpour,Hossein Darvish,Babak Emamalizadeh	2018	9
14	Support for “Disease-Only” Genotypes and Excess of Homozygosity at the CYTH4 Primate-Specific GTTT-Repeat in Schizophrenia Ehteram Khademi,Elham Alehabib,Ehsan Esmaili Shandiz,Azadeh Ahmadifard,Monavvar Andarva,Javad Jamshidi,Simin Rahimi-Aliabadi,Ramin Pouriran,Farhad Ramezani Nejad,Nader Mansoori,Neda Shahmohammadibeni,Shaghyegh Taghavi,Parasto Shokraeian,Haleh Akhavan‐Niaki,Coro Paisán‐Ruiz,Hossein Darvish,Mina Ohadi	2017	14
15	c.376G>A mutation in WFS1 gene causes Wolfram syndrome without deafness Behnam Safarpour Lima,Hamid Ghaedi,Narsis Daftarian,Hamid Ahmadieh,Javad Jamshidi,Mehdi Khorrami,Rezvan Noroozi,Nasim Sohrabifar,Farhad Assarzadegan,Omid Hesami,Shaghayegh Taghavi,Azadeh Ahmadifard,Minoo Atakhorrami,Simin Rahimi-Aliabadi,Neda Shahmohammadibeni,Elham Alehabib,Monavvar Andarva,Hossein Darvish,Babak Emamalizadeh	2016	6
16	Genetic Analysis of the ZNF512B , SLC41A1, and ALDH2 Polymorphisms in Parkinson's Disease in the Iranian Population Faranak Madadi,Mahmoud Shekari Khaniani,Ehsan Esmaili Shandiz,Hormoz Ayromlou,Safa Najmi,Babak Emamalizadeh,Shaghayegh Taghavi,Javad Jamshidi,Abbas Tafakhori,Gholam Ali Shahidi,Hossein Darvish	2016	13
17	SNAP-25gene variations and attention-deficit hyperactivity disorder in Iranian population Mahjoubeh Zarrabi Alhosseini,Javad Jamshidi,Alireza Zare Bidoki,Saeid Ganji,M. R. Eslami,Babak Emamalizadeh,Shaghayegh Taghavi,Parasto Shokraeian,Fatemeh Mohajerani,Hossein Darvish	2016	1
18	FABP9 Mutations Are Not Detected in Cases of Infertility due to Sperm Morphological Defects in Iranian Men Javad Jamshidi,Farkhondeh Pouresmaeili,Hossein Darvish,Mir Davood Omrani,Eznollah Azargashb,Mohammad Reza Sadeghi,Niknam Lakpour	2014	2
19	The structure Biology and Application of Phytohemagglutinin (PHA) in Phytomedicine: With special up-to-date references to lectins Abolfazl Movafagh,Kiandokht Ghanati,Davar Amani,Seyed Mohammad Mahdavi,Mehrdad Hashemi,Davood Zare Abdolahi,Hossein Darvish,Milad Gholami,Leyla HaghNejad,Sara Mosammami,Shamsi Safari,Reyhaneh Darehgazani,Mehrali Rahimi,Nilofar Safavi Naini,Mehdi Ghandehari Motlagh,Mahdi Zamani	2013	9
20	Identification of homogeneously staining regions in leukemia patients Mohammad Heydarian Moghadam,Abolfazl Movafagh,Mirdavood Omrani,Kiandokht Ghanati,Mehrdad Hashemi,Farhikhteh Poursafavi,Hossein Darvish,Davood Zare Abdolahi,Milad Gholami,Mohammad Reza Heidari Rostamy,Shamsi Safari,Leyla HaghNejad,Reyhaneh Darehgazani,Niloofar Safavi Naeini,Mehdi Ghandehari Motlagh,Davar Amani	2013	1

About Hossein Darvish

Hossein Darvish is a scholar working on Genetics, Cell Biology and Neurology, having authored 96 papers that have together received 1.3k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (22 papers), Autism Spectrum Disorder Research (12 papers), Genomics and Rare Diseases (10 papers), Parkinson's Disease Mechanisms and Treatments (10 papers), Genomic variations and chromosomal abnormalities (9 papers), RNA Research and Splicing (9 papers), RNA regulation and disease (7 papers) and RNA and protein synthesis mechanisms (6 papers). The work is most often cited by research in Neurology (259 citations), Neurology (129 citations) and Cellular and Molecular Neuroscience (270 citations). Hossein Darvish has collaborated with scholars based in Iran, United States and Germany. Frequent co-authors include Coro Paisán‐Ruiz, Mina Ohadi, Abbas Tafakhori, Gholam Ali Shahidi, Babak Emamalizadeh, Javad Jamshidi, Siamak Karkheiran, Ruth H. Walker, Vladimir Makarov and Catharine E. Krebs.

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